abnormality of the spinal cord Gene Set

Dataset GWASdb SNP-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0002143
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Genes

15 genes associated with the abnormality of the spinal cord phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol Name Standardized Value
ADARB2 adenosine deaminase, RNA-specific, B2 (non-functional) 0.876787
IL22RA2 interleukin 22 receptor, alpha 2 0.868241
CNTNAP2 contactin associated protein-like 2 0.825497
BRPF3 bromodomain and PHD finger containing, 3 0.802966
CYP7A1 cytochrome P450, family 7, subfamily A, polypeptide 1 0.802966
KCNH1 potassium channel, voltage gated eag related subfamily H, member 1 0.7965
DPYD dihydropyrimidine dehydrogenase 0.767696
ATP7B ATPase, Cu++ transporting, beta polypeptide 0.726078
ADRA1A adrenoceptor alpha 1A 0.714661
TNFRSF11A tumor necrosis factor receptor superfamily, member 11a, NFKB activator 0.703894
UTP14C UTP14, U3 small nucleolar ribonucleoprotein, homolog C (yeast) 0.700393
NCK2 NCK adaptor protein 2 0.687523
ALG11 ALG11, alpha-1,2-mannosyltransferase 0.684556
SPACA7 sperm acrosome associated 7 0.681679
FHL3 four and a half LIM domains 3 0.669923